Dissecting the biological functions of Drosophila histone deacetylases by RNA interference and transcriptional profiling.
Articolo
Data di Pubblicazione:
2006
Abstract:
Zinc-dependent histone deacetylases (HDACs) are a family of
hydrolases first identified as components of transcriptional repressor
complexes, where they act by deacetylating lysine residues at the
N-terminal extensions of core histones, thereby affecting transcription.
To get more insight into the biological functions of the individual
HDAC family members, we have used RNA interference in
combination with microarray analysis in Drosophila S2 cells.
Silencing of Drosophila HDAC1 (DHDAC1), but not of the other
DHDAC family members, leads to increased histone acetylation.
Silencing of either DHDAC1 or DHDAC3 leads to cell growth inhibition
and deregulated transcription of both common and distinct
groups of genes. Silencing DHDAC2 leads to increased tubulin
acetylation levels but was not associated with a deregulation of gene
expression. No growth of phenotype and no significant deregulation
of gene expression was observed upon silencing of DHDAC4
andDHDACX. Loss of DHDAC1 or exposure of S2 cells to the small
molecule HDAC inhibitor trichostatin both lead to a G2 arrest and
were associated with significantly overlapping gene expression signatures
in which genes involved in nucleobase and lipid metabolism,
DNAreplication, cell cycle regulation, and signal transduction
were over-represented. A large number of these genes were shown
to also be deregulated upon loss of the co-repressor SIN3 (Pile, L. A.,
Spellman, P. T., Katzenberger, R. J., and Wassarman, D. A. (2003)
J. Biol. Chem. 278, 37840-37848). We conclude the following. 1)
DHDAC1 and -3 have distinct functions in the control of gene
expression. 2) Under the tested conditions, DHDAC2, -4, and X
have no detectable transcriptional functions in S2 cells. 3) The antiproliferative
and transcriptional effects of trichostatin are largely
recapitulated by the loss of DHDAC1. 4) The deacetylase activity of
DHDAC1 significantly contributes to the repressor function of
SIN3
Tipologia CRIS:
01.01 Articolo in rivista
Elenco autori:
Cundari, Enrico
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